Tegaserod til behandling af kvinder med colon irritabile

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Abstract

Irritable bowel syndrome (IBS) is a chronic, relapsing disease characterised by abdominal pain and altered bowel movements. This review assesses the clinical trials of the partial serotonin receptor agonist tegaserod in women with constipation type IBS. Significantly more women treated with tegaserod obtained sufficient relief from symptoms during at least 2 out of 4 weeks, but the absolute therapeutic gain of approximately 10 percent was not deemed clinically relevant. Two marketing authorisation applications in the European Union have been rejected due to the minor therapeutic gain. Tegaserod was removed from the market in the USA in March 2007 due to an increased risk of severe cardiovascular adverse events.

Bidragets oversatte titelTegaserod in treatment of women with irritable bowel syndrome
OriginalsprogDansk
TidsskriftUgeskrift for Læger
Vol/bind169
Udgave nummer23
Sider (fra-til)2190-2
Antal sider3
ISSN0041-5782
StatusUdgivet - 4. jun. 2007
Udgivet eksterntJa

Emneord

  • Constipation/drug therapy
  • Evidence-Based Medicine
  • Female
  • Gastrointestinal Agents/adverse effects
  • Humans
  • Indoles/adverse effects
  • Irritable Bowel Syndrome/drug therapy
  • Randomized Controlled Trials as Topic
  • Serotonin Receptor Agonists/adverse effects
  • Treatment Outcome

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